Seckel syndrome with polyarteritis nodosa

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dc.authorscopusid7003405757
dc.authorscopusid7006266098
dc.authorscopusid6603164230
dc.authorscopusid55928547600
dc.contributor.authorKutlu R.
dc.contributor.authorAlkan A.
dc.contributor.authorKutlu O.
dc.contributor.authorYakinci C.
dc.date.accessioned2024-08-04T19:59:07Z
dc.date.available2024-08-04T19:59:07Z
dc.date.issued2004
dc.departmentİnönü Üniversitesien_US
dc.description.abstractSeckel syndrome is a rare genetic disorder with a typical "bird-headed" appearance. It could affect many organ systems but renal involvement is uncommon. Polyarteritis nodosa is systemic vasculitic disorder which also involves kidneys. We report a case of Seckel syndrome in a 9 year-old boy with renal involvement due to polyarteritis nodosa. According to the literature, this is the first report of polyarteritis nodosa in Seckel syndrome.en_US
dc.identifier.endpage1161en_US
dc.identifier.issn0019-6061
dc.identifier.issue11en_US
dc.identifier.pmid15591669en_US
dc.identifier.scopus2-s2.0-9344239397en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage1158en_US
dc.identifier.urihttps://hdl.handle.net/11616/90410
dc.identifier.volume41en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofIndian Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPolyarteritis nodosaen_US
dc.subjectSeckel syndromeen_US
dc.titleSeckel syndrome with polyarteritis nodosaen_US
dc.typeArticleen_US

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